prednisolone acetate
Generic: prednisolone acetate
Labeler: a-s medication solutionsDrug Facts
Product Profile
Brand Name
prednisolone acetate
Generic Name
prednisolone acetate
Labeler
a-s medication solutions
Dosage Form
SUSPENSION/ DROPS
Routes
Active Ingredients
prednisolone acetate 10 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
50090-0559
Product ID
50090-0559_54821cc4-1238-4ab7-926f-4e6a185d55e5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA AUTHORIZED GENERIC
Application Number
NDA017469
Listing Expiration
2026-12-31
Marketing Start
1994-12-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
500900559
Hyphenated Format
50090-0559
Supplemental Identifiers
RxCUI
UNII
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
prednisolone acetate (source: ndc)
Generic Name
prednisolone acetate (source: ndc)
Application Number
NDA017469 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 10 mg/mL
Packaging
- 1 BOTTLE, PLASTIC in 1 CARTON (50090-0559-0) / 10 mL in 1 BOTTLE, PLASTIC
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "54821cc4-1238-4ab7-926f-4e6a185d55e5", "openfda": {"unii": ["8B2807733D"], "rxcui": ["1376336"], "spl_set_id": ["b1d30a4f-4941-45a5-bd24-fea07f1bfc87"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, PLASTIC in 1 CARTON (50090-0559-0) / 10 mL in 1 BOTTLE, PLASTIC", "package_ndc": "50090-0559-0", "marketing_start_date": "20160629"}], "brand_name": "Prednisolone Acetate", "product_id": "50090-0559_54821cc4-1238-4ab7-926f-4e6a185d55e5", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Corticosteroid Hormone Receptor Agonists [MoA]", "Corticosteroid [EPC]"], "product_ndc": "50090-0559", "generic_name": "Prednisolone Acetate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prednisolone Acetate", "active_ingredients": [{"name": "PREDNISOLONE ACETATE", "strength": "10 mg/mL"}], "application_number": "NDA017469", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "19941215", "listing_expiration_date": "20261231"}